Literature DB >> 5546784

[A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].

P Boivin, C Galand, J Hakim, D Simony, M Seligman.   

Abstract

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Year:  1971        PMID： 5546784

Source DB:  PubMed          Journal:  Presse Med        ISSN： 0032-7867            Impact factor:   1.228


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  5 in total

1.  Uridine monophosphate kinase: A new genetic polymorphism with possible clinical implications.

Authors:  E R Giblett; J E Anderson; S H Chen; Y S Teng; F Cohen
Journal:  Am J Hum Genet       Date:  1974-09       Impact factor: 11.025

Review 2.  [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].

Authors:  H D Waller; H C Benöhr
Journal:  Klin Wochenschr       Date:  1976-09-01

3.  Inborn errors of purine metabolism: clinical update and therapies.

Authors:  Shanti Balasubramaniam; John A Duley; John Christodoulou
Journal:  J Inherit Metab Dis       Date:  2014-06-28       Impact factor: 4.982

4.  Metabolic compensation for profound erythrocyte adenylate kinase deficiency. A hereditary enzyme defect without hemolytic anemia.

Authors:  E Beutler; D Carson; H Dannawi; L Forman; W Kuhl; C West; B Westwood
Journal:  J Clin Invest       Date:  1983-08       Impact factor: 14.808

5.  Red cell adenylate kinase deficiency in China: molecular study of 2 new mutations (413G > A, 223dupA).

Authors:  Sijia He; Hongbo Chen; Xia Guo; Ju Gao
Journal:  BMC Med Genomics       Date:  2022-05-04       Impact factor: 3.622
  5 in total

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